Butane, 1,4-diiodo-2-methyl- CAS:66688-32-2 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating resear
Cas:66688-32-2
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:66688-32-2
Min.Order:10 Gram
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Cas:66688-32-2
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inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
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inquiryButane, 1,4-diiodo-2-methyl-Appearance:Off white to slight yellow solid Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By c
Manufacturer,strong R&D,professional team Storage:Store in a cool, dry place. Store in a tightly closed container. Package:according to your requirement Application:ZhiShang Chemical is owned by ZhiShang Group, is a professional new-type chemicals en
1,4-dibromo-2-methyl-butane
1,4-diiodo-2-methylbutane
Conditions | Yield |
---|---|
With sodium iodide In acetone Ambient temperature; | 99% |
3-methyltetrahydrofuran
1,4-diiodo-2-methylbutane
Conditions | Yield |
---|---|
With O-phenyl phosphorodichloridate; sodium iodide for 40h; Heating; | 85% |
Diethyl difluoromethylphosphonate
1,4-diiodo-2-methylbutane
A
diethyl 1,1-difluoro-5-iodo-4-methylpentylphosphonate
Conditions | Yield |
---|---|
Stage #1: Diethyl difluoromethylphosphonate With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 1.16667h; Stage #2: 2-methyl-1,4-diiodobutane In tetrahydrofuran at -78℃; for 4h; | A 30% B 7% |
tert-butyl (trimethylsilyl)acetate
1,4-diiodo-2-methylbutane
tert-butyl 1-(trimethylsilyl)-3-methylcyclopentanecarboxylate
Conditions | Yield |
---|---|
With lithium diisopropyl amide 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight; Yield given. Multistep reaction; |
1,4-diiodo-2-methylbutane
3-methyltetrahydrothiophene
Conditions | Yield |
---|---|
With sodium sulfide In ethanol; water for 6h; Heating; Yield given; |
1,4-diiodo-2-methylbutane
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: lithium diisopropylamide / tetrahydrofuran / 1.17 h / -78 °C 1.2: 30 percent / tetrahydrofuran / 4 h / -78 °C 2.1: 52 percent / potassium carbonate / dimethylformamide / 20 °C 3.1: bromotrimethylsilane / CH2Cl2 / 44 h / 20 °C View Scheme |
1,4-diiodo-2-methylbutane
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: lithium diisopropylamide / tetrahydrofuran / 1.17 h / -78 °C 1.2: 30 percent / tetrahydrofuran / 4 h / -78 °C 2.1: 52 percent / potassium carbonate / dimethylformamide / 20 °C 3.1: bromotrimethylsilane / CH2Cl2 / 44 h / 20 °C 4.1: hydrochloric acid / Heating View Scheme |
1,4-diiodo-2-methylbutane
diethyl 5-(6-chloro-9H-purin-9-yl)-1,1-difluoro-4-methylpentylphosphonate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: lithium diisopropylamide / tetrahydrofuran / 1.17 h / -78 °C 1.2: 30 percent / tetrahydrofuran / 4 h / -78 °C 2.1: 52 percent / potassium carbonate / dimethylformamide / 20 °C View Scheme |
1,4-diiodo-2-methylbutane
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: lithium diisopropylamide / tetrahydrofuran / 1.17 h / -78 °C 1.2: 30 percent / tetrahydrofuran / 4 h / -78 °C 2.1: 37 percent / potassium carbonate / dimethylformamide / 23 h / 20 °C 3.1: bromotrimethylsilane / CH2Cl2 / 44 h / 20 °C View Scheme |
1,4-diiodo-2-methylbutane
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: lithium diisopropylamide / tetrahydrofuran / 1.17 h / -78 °C 1.2: 30 percent / tetrahydrofuran / 4 h / -78 °C 2.1: 37 percent / potassium carbonate / dimethylformamide / 23 h / 20 °C 3.1: bromotrimethylsilane / CH2Cl2 / 44 h / 20 °C 4.1: 388 mg / hydrochloric acid / Heating View Scheme |
1,4-diiodo-2-methylbutane
diethyl 5-(2-amino-6-chloro-9H-purin-9-yl)-1,1-difluoro-4-methylpentylphosphonate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: lithium diisopropylamide / tetrahydrofuran / 1.17 h / -78 °C 1.2: 30 percent / tetrahydrofuran / 4 h / -78 °C 2.1: 37 percent / potassium carbonate / dimethylformamide / 23 h / 20 °C View Scheme |
1,4-diiodo-2-methylbutane
3-methyl-thiolane-1-oxide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Na2S*9H2O / ethanol; H2O / 6 h / Heating 2: 51 percent / NaIO4 / H2O / 0 °C View Scheme |
1,4-diiodo-2-methylbutane
Trimethyl-((1R,3R)-3-methyl-cyclopentyl)-silane
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: 1.) LDA / 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight 2: 1.29 g / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C 3: 83 percent / Ag2CO3, Celite / benzene / 7 h / Heating 4: 1.89 g / diethyl ether / 0.33 h / -78 °C 5: CrO3, pyridine / CH2Cl2 / 0.67 h 6: NaNH2 / benzene / 2 h / Ambient temperature View Scheme |
1,4-diiodo-2-methylbutane
Trimethyl-((1R,3S)-3-methyl-cyclopentyl)-silane
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: 1.) LDA / 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight 2: 1.29 g / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C 3: 83 percent / Ag2CO3, Celite / benzene / 7 h / Heating 4: 1.89 g / diethyl ether / 0.33 h / -78 °C 5: CrO3, pyridine / CH2Cl2 / 0.67 h 6: NaNH2 / benzene / 2 h / Ambient temperature View Scheme |
1,4-diiodo-2-methylbutane
cis-1-(trimethylsilyl)-3-methylcyclopentanemethanol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) LDA / 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight 2: 1.40 g / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C View Scheme |
1,4-diiodo-2-methylbutane
trans-1-(trimethylsilyl)-3-methylcyclopentanemethanol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) LDA / 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight 2: 1.29 g / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C View Scheme |
1,4-diiodo-2-methylbutane
(1R,3R)-3-Methyl-1-trimethylsilanyl-cyclopentanecarbaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1.) LDA / 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight 2: 1.40 g / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C 3: 85 percent / Ag2CO3, Celite / benzene / 7 h / Heating View Scheme |
1,4-diiodo-2-methylbutane
(1R,3S)-3-Methyl-1-trimethylsilanyl-cyclopentanecarbaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1.) LDA / 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight 2: 1.29 g / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C 3: 83 percent / Ag2CO3, Celite / benzene / 7 h / Heating View Scheme |
1,4-diiodo-2-methylbutane
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 1.) LDA / 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight 2: 1.40 g / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C 3: 85 percent / Ag2CO3, Celite / benzene / 7 h / Heating 4: 2.10 g / diethyl ether / 0.33 h / -78 °C View Scheme |
1,4-diiodo-2-methylbutane
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 1.) LDA / 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight 2: 1.29 g / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C 3: 83 percent / Ag2CO3, Celite / benzene / 7 h / Heating 4: 1.89 g / diethyl ether / 0.33 h / -78 °C View Scheme |
1,4-diiodo-2-methylbutane
trans-1-benzoyl-1-(trimethylsilyl)-3-methylcyclopentane
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 1.) LDA / 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight 2: 1.40 g / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C 3: 85 percent / Ag2CO3, Celite / benzene / 7 h / Heating 4: 2.10 g / diethyl ether / 0.33 h / -78 °C 5: CrO3, pyridine / CH2Cl2 / 0.67 h View Scheme |
1,4-diiodo-2-methylbutane
cis-1-benzoyl-1-(trimethylsilyl)-3-methylcyclopentane
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 1.) LDA / 1.) THF, -78 deg C, 15 min, 2.) a) -30 deg C, 3 h, b) 20 deg C, overnight 2: 1.29 g / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C 3: 83 percent / Ag2CO3, Celite / benzene / 7 h / Heating 4: 1.89 g / diethyl ether / 0.33 h / -78 °C 5: CrO3, pyridine / CH2Cl2 / 0.67 h View Scheme |
4-hydroxy-3,5-di-tert-butylthiophenol
1,4-diiodo-2-methylbutane
sulfur
Conditions | Yield |
---|---|
Stage #1: 4-hydroxy-3,5-di-tert-butylthiophenol; 4-amino-4'-ethyldiphenylamine; 2-methyl-1,4-diiodobutane With potassium carbonate In toluene at 90℃; for 3h; Inert atmosphere; Stage #2: sulfur With iodine In toluene at 20 - 150℃; for 8h; Inert atmosphere; |
4-hydroxy-3,5-di-tert-butylthiophenol
1,4-diiodo-2-methylbutane
Conditions | Yield |
---|---|
With potassium carbonate In toluene at 90℃; for 3h; Inert atmosphere; |
4-hydroxy-3,5-di-tert-butylthiophenol
4-amino-4'-ethyl-N,N-diphenylamine
1,4-diiodo-2-methylbutane
Conditions | Yield |
---|---|
Stage #1: 4-hydroxy-3,5-di-tert-butylthiophenol; 4-amino-4'-ethyl-N,N-diphenylamine; 2-methyl-1,4-diiodobutane With potassium carbonate In toluene at 90℃; for 3h; Inert atmosphere; Stage #2: With iodine; sulfur In toluene at 150℃; for 8h; Inert atmosphere; |
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